Fluorinated triazine monomers

ABSTRACT

A compound of formula (I), wherein R 1  and R 2  are independently selected from saturated fluorocarbon substituted side chains, such as NR 5 (CH 2 ) n C m F 2m+1 , O(CH 2 ) n C m F 2m+1 , S(CH 2 ) n C m F 2m+1 , NR 5 S(O) 2 (CH 2 ) p C m F 2m+1 , or CR 5 [CO 2 (CH 2 ) n C m F 2m+1 ] 2 , where R 5  is hydrogen or alkyl, n and m are independently an integer of 1-12, and p is 0 or an integer of 1-12, R 3  is an unsaturate moiety which may be polymerised, and X is O, S or NR 4  where R 4  is hydrogen or alkyl, as well as methods for the preparation of these compounds. Compounds of formula (I) are useful monomers in the preparation of oil- and water-repellent polymers.

The present invention relates to novel monomeric compounds which can be used in the production of polymers which have a high degree of oil and water-repellency and which may be fixed to substrates such as clothing, to processes for their preparation and to polymers produced therefrom.

Oil- and water-repellent treatments are in widespread use, in particular for outdoor clothing applications, sportswear, leisurewear and in military applications. These treatments generally require the incorporation of a fluoropolymer into or more particularly, fixed onto the surface of the clothing fabric. The degree of oil and water repellency is a function of the number of fluorocarbon groups or moieties that can be fitted into the available space. The greater the concentration of such moieties, the greater the repellency of the finish.

In addition however, the polymeric compounds must be able to form durable bonds with the substrate. Oil- and water-repellent textile treatments are generally based on fluoropolymers that are applied to fabric in the form of an aqueous emulsion. The fabric remains breathable and permeable to air since the treatment simply coats the fibres with a very thin, liquid-repellent film. In order to make these finishes durable, they are sometimes co-applied with cross-linking resins that bind the fluoropolymer treatment to fibres. Whilst good levels of durability towards laundering and dry-cleaning can be achieved in this way, the cross-linking resins can seriously damage cellulosic fibres and reduce the mechanical strength of the material. WO 97/13024 discloses a group of fibre reactive polymers, which include a functional group such as a triazine group, which binds the polymer to the material substrate.

British patent No 1,102,903 describes certain fluoro alkyl containing compounds which are used in water- and oil-repellent compositions.

The applicants have produced certain novel monomers, which give rise to polymers which have a high number of fluorocarbon substituents per monomer unit.

The present invention provides a compound of formula (I)

wherein R¹ and R² are independently selected from saturated fluorocarbon substituted side chains;

R³ is an unsaturated moiety which may be polymerised, and X is O, S or NR⁴ where R⁴ is hydrogen or alkyl.

As used herein, the term “alkyl” refers to straight or branched chain alkyl or cycloalkyl groups, in particular those having from 1 to 12 and preferably from 1 to 6 carbon atoms. The term “saturated” refers to groups which do not contain carbon-carbon double bonds. Conversely the term “unsaturated” refers to groups which include carbon-carbon double bonds.

Suitable fluorocarbon substituted side chains for R¹ and/or R² include groups which are hydrophobic groups which are able to confer water- and/or oil- repellency on the resultant polymer. In particular R¹ and R² are independently selected from NR⁵(CH₂)_(n)C_(m)F_(2m+1), O(CH₂)_(n)C_(m)F_(2m+1), S(CH₂)_(n)C_(m)F_(2m+1), NR⁵S(O)₂(CH₂)_(p)C_(m)F_(2m+1) or CR⁵[CO₂(CH₂)_(n)C_(m)F_(2m+1)]₂, where R⁵ is hydrogen or alkyl, and n and m are independently an integer of 1-12, and p is 0 or an integer of from 1-12.

Conveniently R¹ and R² are the same. They are preferably selected from O(CH₂)_(n)C_(m)F_(2m+1) or NR⁵S(O)₂(CH₂)_(p)C_(m)F_(2m+1). Suitably R⁵ is methyl, ethyl or n-propyl, in particular ethyl. Preferred integers for n and p are from 1-3, suitably 2, whilst preferred integers for m are from 6 to 10, most preferably 8.

Suitable polymerisable groups R³ are alkenes or alkynes which may also include a functional group such as an acyloxy group. Particularly preferred groups for R³ are groups of formula (CH₂)_(q)OC(O)C(R⁶)CR⁷R⁸ where q is an integer of from 1 to 12, suitably from 1 to 4 and especially 2, and R⁶, R⁷ and R⁸ are independently selected from hydrogen or alkyl such as C₁₋₄ alkyl. Preferably R⁶, R⁷ and R⁸ are all hydrogen.

Compounds of formula (I) are suitably prepared by reacting a compound of formula (II)

where R¹ and R² are as defined in relation to formula (I) and Y is a leaving group, with a group of formula (III)

 R^(a)—X—R^(3′)  (III)

where X is as defined in relation to formula (I) and R³ is a group R³ as defined in relation to formula (I) or a precursor group which may be reacted to form a group R³ and R⁸ is hydrogen or alkyl; and thereafter if necessary converting a precursor group R³ to a group R³.

Preferably R^(a) is hydrogen or a lower alkyl, for example a C₁₋₃ alkyl, in particular methyl.

Suitable leaving groups for Y include halogen such as fluorine and chlorine, in particular chlorine, or amine leaving groups such as substituted pyridines for instance nicotinic acid or colladine.

The reaction is suitably effected in an organic solvent such as tetrahydrofuran (THF), acetone, toluene or chloroform. It may be effected at temperatures of from 0 to 200° C., suitably from 25 to 150° C., depending upon the precise nature of the reactants and solvents involved. Conveniently the reaction may be effected at room temperature or under reflux conditions.

Preferably the reaction is effected under basic conditions. Weak bases may suffice, and in some instances, the compound of formula (III) may itself act as an acid scavenger and so the use of an excess, particularly a 2 molar excess of the compound of formula (III) will ensure that that the reaction proceeds effectively.

Suitable groups R³′ which are precursor groups to R³ would be apparent to the skilled person. For example, where R³ is a group (CH₂)_(q)OC(O)C(R⁶)CR⁷R⁸, a suitable precursor group R³ would be (CH₂)_(q)OH, which can be readily converted to R³ by reaction with a suitable acid halide for example an acid chloride of formula ClC(O)C(R⁶)CR₇R⁷ in the presence of a base, such as a weak base, for example pyridine or a pyridine derivative such as collidine. This reaction is suitably effected in an organic solvent such as toluene at elevated temperatures, conveniently at the reflux temperature of the solvent.

Certain compounds of formula (II) are known (see for example British Patent No. 1,102,903). These compounds can be prepared by reacting a compound of formula (IV)

where R¹ is as defined in relation to formula (I), Y is as defined in relation to formula (II) and Y′ is a leaving group,

with a compound of formula (V)

R²H  (V)

where R² is as defined in relation to formula (I), in the presence of a base.

Suitable bases are those which react with a compound of formula (V) so as to produce a nucleophilic moiety of formula (V′)

(R²)⁻  (V′)

Thus the selection of suitable bases will depend upon the precise nature of the group R² and will be readily understood or determinable by the skilled person. For example, where R² is a group O(CH₂)_(n)C_(m)F_(2m+1), strong bases such as alkali metal hydroxides, in particular lithium hydroxide, may be used. Alternatively, where R² is a group NR⁵S(O)₂(CH₂)_(p)C_(m)F_(2m+1), stronger bases such as alkali metal alkoxides, in particular sodium or potassium methoxide or ethoxide may be used.

Compounds of formula (IV) are suitably prepared by reacting a compound of formula (VI)

wherein Y, Y′and Y″ are the same or different leaving groups, with a compound of formula (VII)

R¹H  (VII)

where R¹ is as defined in relation to formula (I), in the presence of a base.

Reaction conditions will be generally similar to those described above in relation to the reaction between compounds of formula (IV) and formula (V).

Where compounds of formula (V) and formula (VII) are the same, compounds of formula (II) may be prepared directly in one pot. If necessary, the reaction can be controlled in a stepwise manner in order to maximise yield of the target compound by controlling the reaction temperature. For example, where R¹ and R² are groups of formula NR⁵S(O)₂(CH₂)_(n)C_(m)F_(2m+1), the compound of formula (IV) may be prepared at depressed temperatures, for example at about −78° C. Allowing the reaction mixture to warm up to approximately 0° C. will produce a compound of formula (II) after suitable work-up.

Compounds of formula (III), (V), (VI) and (VII) are either known compounds or they can be prepared from known compounds using conventional methods. A preferred compound of formula (VI) is cyanuric chloride.

Compounds of formula (I) may be polymerised or copolymerised using conventional technology, e.g emulsion polymerisation.

Polymers or copolymers including units of formula (VIII)

where R¹, R² and X are as defined in relation to formula (I), t is an integer in excess of 5, and R⁹ is a saturated derivative of R³ as defined in relation to formula (I) form a preferred embodiment of the invention.

In particular XR⁹ will be a moiety of formula (IX)

Suitably the monomers of the invention are copolymerised with a monomer which comprises a fibre reactive moiety for example as described in WO 97/13024.

The invention will now be particularly described by way of example.

EXAMPLE 1 Step 1 Synthesis of 2-chloro-4,6-bis(N-Ethylperfluorooctylsulphonamido)-1,3,5-triazine

Metallic sodium (4.08 g, 177 mmols) was reacted with methanol (150 mls). N-Ethyl perfluorooctyl sulphonamide (93.28 g, 177 mmols) was added, and the resulting solution was stirred for 30 minutes. The methanol was removed at the pump (a vacuum pump was required to remove the final traces of solvent). The resulting sticky solid was dissolved in acetone (300 mls) and cooled to −65° C. under argon. Recrystalised cyanuric chloride (16.33 g, 88.5 mmols) dissolved in acetone (100 mls) was added to the reaction mixture dropwise such that the temperature did not rise above −50° C. (˜1 hour). After the addition, the reaction mixture was allowed to slowly warm to room temperature (1 hour) and then stirred for a further 3 hours. The precipated solid was removed by filtration and dried under vacuum. Purification by soxhlet extraction with acetone afforded 61 g (56.9%) of a fine white powder.

¹H NMR (CDCl₃) δ (ppm) 4.20 (2H, q, ³J_(H-H) 6.8 Hz, CH ₂CH₃), 1.40 (3H, t, ³J_(H-H) 6.8 Hz, CH₂ CH ₃) ¹³C{¹H} NMR (CDCl₃) δ (ppm) 171.3, 165.0 (triazine), 46.3 (CH ₂CH₃), 14.5 (CH₂ CH ₃).

Step 2 Synthesis of 2-N-{4,6-bis(N-ethylperfluorooctylsulphonamido)-1,3,5-triazin-2-yl}-amino Ethanol

A THF solution (85 mls) of 2-chloro-4,6-bis(N-ethylperfluorooctylsulphonamido)-1,3,5-triazine (15 g, 12.9 mmols) and ethanolamine (1.6 g, 26.2 mmols) were heated under reflux for 1 hour. The hot solution/suspension was filtered and the product was allowed to crystalise overnight to afford 12.8 g (83%) of product.

¹H NMR (d₆acetone) δ (ppm) 4.85 (4H, m, NCH ₂CH₃), 4.38 (2H, t, ³J_(H-H) 5 Hz, CH₂O), 4.22 (2H, dt, 5, 5 Hz, OCH₂ CH ₂N), 2.05 (6H, m NCH₂ CH ₃).

Step 3 Synthesis of 2-N-{(4,6-bis(N-Ethylperfluorooctylsulphonamido)-1,3,5-triazin-2-yl)}-aminoethyl Propenoate

2-N-[4,6-bis(N-ethylperfluorooctylsulphonamido)-1,3,5-triazin-2-yl]amino ethanol (11.58, 9.7 mmols) and acryloyl chloride (1.32 g, 14.6 mmols) were dissolved in hot toluene (80 mls). Collidine (1.77 g, 14.6 mmols) was added as a toluene solution (10 mls) down the reflux condenser. The resulting reaction mixture was heated under reflux for 2 hours and then filtered hot. Toluene was removed at the pump and the resulting solid dissolved in diethyl ether (400 mls). The etheral solution was washed with 1M HCl (2×50 mls) distilled water (2×40 mls) and then dried over sodium sulphate. Filtration and evaporation of the solvent at the pump afforded 8.8 g (73%) of product.

¹H NMR (CDCl₃) δ (ppm) 6.42 (1H, dd, ³J_(H-H) 17.3, 1.3 Hz, CH═CH _(2 trans)), 6-11 (1H, dd, 3J_(H-H) 17.3, 10.5 Hz, CH═CH₂), 5.88 (2H, m, NH, CH═CH _(2 cia) ), 4.32 (2H, t, ³J_(H-H) 5.3 Hz, CH₂O), 4.13 (4H, m, NCH ₂CH₃), 3.72 (2H, m, OCH₂ CH ₂N), 1.36 (6H, m, NCH₂ CH ₃).

¹³C{¹H} NMR (CDCl₃) δ (ppm) 166.0, 165.6, 164.6, 164.3, (triazine/C═O), 131.5 (C═C), 127.8 (C═C), 62.5 (CH ₂O), 45.4 (CH₃ CH ₂N), 40.5 (CH ₂N), 14.9 (CH ₃CH₂).

EXAMPLE 2 Synthesis of 2-[N-Methyl-N-{(4,6-bis(N-ethylperfluorooctylsulphonamido)-1,3,5-triazin-2-yl)}]-aminoethyl Propenoate

2-Chloro-4,6-bis(N-ethylperfluorooctylsulphonamido-) 1,3,5-triazine (20 g, 17.2 mmols) was held as a solution/suspension in chloroform (150 mls). N,N-Dimethylethylamino acrylate (2.459, 17.2 mmols) was added dropwise, over a period of 30 minutes, as a chloroform solution (50 mls). The reaction mixture was stirred for 3 hours at room temperature. The chloroform solution was filtered through Celite®, concentrated (to a volume of approximately 30 mls) and then passed through a short path column of silica. Product was eluted with chloroform. Evaporation of the solvent afforded 19 g (88%) of a sticky oil that crystalised with time (2 days).

¹H NMR (CDCl₃) δ (ppm) 6.37 (1H, dd, ³J_(H-H) 17.3, 1.5 Hz, CH═CH _(2 trans)), 6.09 (1H, dd, ³J_(H-H) 17.3, 10.5 Hz, CH═CH₂), 5.83 (1H, dd, ³J_(H-H) 10.5, 1.5 Hz, CH═CH _(2 cis) ), 4.36 (2H, t, ³J_(H-H) 5.6 Hz, CH₂O), 4.14 (4H, m, NCH ₂CH₃), 3.86 (2H, t, ³J_(H-H) 5.6 Hz, OCH₂ CH ₂N), 3.20 (3H, S, CH₃N), 1.38 (6H, m, NCH₂ CH ₃). ¹³C{¹H} NMR (CDCl₃) δ (ppm) 165.8, 164.5, 164.2, 164.0, (triazine/C═O), 131.3 (C═C), 127.9 (C═C), 61.7 (CH ₂O), 48.3 (CH ₂N), 45.5 (CH ₂N), 36.3 (CH₃N), 15.0 (CH ₃CH₂).

EXAMPLE 3 Step 1 Synthesis of 2,4-bis(1H,1H,2H,2H-Perfluorootoxy)-6-chloro-1,3,5-triazine

Lithium hydroxide (0.49 g, 11.7 mmols) and 1H, 1H, 2H, 2H perfluorooctanol (5.4 g 11.7 mmols) were held as a solution/suspension in tetrahydrofuran (25 mls). Cyanuric chloride (1.08 g, 5.8 mmols) and distilled water (1 ml) were added and the reaction mixture was stirred at room temperature overnight. The resulting solution/suspension was precipitated into distilled water (200 mls) and extracted with diethyl ether (2×200 mls). The organic extract was dried over sodium sulphate, filtered and the diethyl ether was removed at the pump. The resulting white solid was recrystalised form diethyl ether (50 mls), to afford 3.3 g (54%) of product.

¹H NMR (CDCl₃) δ (ppm) 4.75 (2H, t, ³J_(H-H) 6.6 Hz, OCH ₂CH₂), 2.63 (2H, tt, ³J_(H-F) 18.1 Hz, ³J_(H-H) 6.6 Hz OCH₂ CH ₂). ¹³C{¹H} NMR (CDCl₃) δ (ppm) 173.2, 171.7 (triazine), 61.1 (OCH ₂CH₂), 30.5 (t, ²J_(C-F) 22.0 Hz OCH₂ CH ₂CF₂).

Step 2 Synthesis of 2-[N-methyl-N-{(4,6-bis(1H,1H,2H,2H-perfluorooctoxy-)1,3,5-triazin-2-yl)}]-aminoethyl Propenoate

2,4-bis(1H,1H,2H,2H-perfluorooctoxy)-6-chloro-1,3,5-triazine (0.5 g, 0.48 mmols) was held as a solution/suspension in chloroform (10 mls). N,N-Dimethylethyl-amino acrylate (0.076 g, 0.53 mmols) was added dropwise as a neat liquid at room temperature and the reaction mixture was stirred for 2 hours. The chloroform solution was extracted with 2M HCl (2×10 mls), distilled water (2×10 mls), dried over sodium sulphate and filtered. Evaporation of the solvent afforded 0.48 g (90%) of product as a waxy solid.

¹H NMR (CDCl₃) δ (ppm) 6.30 (1H, d, ³J_(H-H) 17.2 Hz, CH═CH_(2 trans)), 6.00 (1H, dd, ³J_(H-H) 17.3, 10.4 Hz, CH═CH₂), 5.75 (1H, d, ³J_(H-H) 10.4 HZ, CH═CH _(2 cis) ), 4.57 (4H, m, CF₂CH₂ CH ₂O), 4.31 (2H, t, 5.5 Hz, OCH ₂CH₂N), 3.84 (2H, t, ³J_(H-H) 5. 5 Hz, OCH₂ CH ₂N), 3.14 (3H, s, CH₃N), 2.56 (4H, m, CF₂ CH ₂CH₂O). ¹³C{¹H} NMR (CDCl₃) δ (ppm) 171.3, 171.1, 167.3, 165.8, (triazine/C═O), 131.1 (C═C), 128.0 (C═C), 61.8 (CH ₂O), 59.2 (CH ₂N), 48.0 (CH ₂N), 36.1 (CH₃N), 30.2 (t, 22 Hz, CH ₂CF₂). 

What is claimed is:
 1. A compound of formula (I)

wherein R¹ and R² are independently selected from NR⁵(CH₂)_(n)C_(m)F_(2m+1), O(CH₂)_(n)C_(m)F_(2m+1), S(CH₂)_(n)C_(m)F_(2m+1), NR⁵S(O)₂(CH₂)_(p)C_(m)F_(2m+1) or CR⁵[CO₂(CH₂)_(n)C_(m)F_(2m=1)]₂, where R⁵ is hydrogen or C₁-C₃ alkyl, n and m are independently an integer of 1-12, and p is 0 or an integer of from 1-12; R³ is an unsaturated moiety which may be polymerized, and X is O, S or NR⁴ where R⁴ is hydrogen or C₁-C₁₂ straight or branched chain alkyl or cycloalkyl.
 2. A compound according to claim 1 wherein R¹ and R² are the same.
 3. A compound according to claim 1 wherein R¹ and R² are selected from O(CH₂)_(n)C_(m)F_(2m+1) or NR⁵S(O)₂(CH₂)_(p)C_(m)F_(2m+1).
 4. A compound according to claim 1 wherein R³ is a group of formula —(CH₂)_(q)OC(O)CR⁶═CR⁷R⁸ where q is an integer of from 1 to 12, and R⁶, R⁷ and R⁸are independently selected from hydrogen or a C₁₋₄ alkyl.
 5. A compound according to claim 4 where R⁶, R⁷ and R⁸ are all hydrogen.
 6. A method of preparing a compound of formula (I) as defined in claim 1, which method comprises reacting a compound of formula (II)

where R¹ and R² are as defined in claim 1 and Y is a leaving group, with a group of formula (III) R^(a)—X—R^(3′)  (III) where X is as defined in claim 1 and R^(3′) is a group R³ as defined in relation to formula (I) or a precursor group which may be reacted to form a group R³ and R^(a) is hydrogen or a C₁₋₃ alkyl group; and thereafter if necessary converting a group R^(3′) to a group R³.
 7. A method according to claim 6 wherein R^(3′) is a group of the formula (CH₂)_(q)OH, and this is subsequently converted to R³ by reaction with an acid halide of formula ZC(O)C(R⁶)═CR⁷R⁸ where Z is a halogen and R⁶, R⁷ and R⁸ are as defined in claim 5, in the presence of a base.
 8. A method according to claim 6 wherein the compound of formula (II) is prepared by reacting a compound of formula (IV)

where R¹ is as defined in relation to formula (I), Y is as defined in relation to formula (II) and Y′ is a leaving group, with a compound of formula (V) R²H  (V) where R² is as defined in relation to formula (I), in the presence of a base.
 9. A method according to claim 8 wherein the compound of formula (IV) is prepared by reacting a compound of formula (VI)

wherein Y, Y′ and Y″ are the same or different leaving groups, with a compound of formula (VII)  R¹H  (VII) where R¹ is as defined in claim 1, in the presence of a base.
 10. A method according to claim 9 wherein the compound of formula (IV) is converted to a compound of formula (II) in situ.
 11. A polymeric compound which has been derived from a compound of formula (I) of claim
 1. 12. A polymeric compound according to claim 11 which comprises a polymer or copolymer including repeating units of formula (VIII)

where R¹, R² and X are define in relation to formula (I), t is an integer in excess of 5, and R⁹ is a saturated derivative of R³ as defined in relation to formula (I).
 13. A polymeric compound according to claim 12 wherein XR^(N) is a moiety of formula (IX)

where q, R⁶, R⁷ and R⁸ are as defined in claim
 4. 14. A substrate which is coated with a polymeric compound according to claim
 11. 15. A substrate according to claim 14 which is a fabric. 